Variant · Snv
DCAF4 NM_015604.4(DCAF4):c.973A>G (p.Ser325Gly)
CI-VAR-00127659Explore in graph →p.Ser325GlyNM_015604.4:c.973A>GClinVar 709977 rs117449182
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 709977 | Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Clear cell carcinoma of kidney; Malignant lymphoma, large B-cell, diffuse; Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Uveal melanoma; Melanoma; Hepatocellular carcinoma; Cervical cancer; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Colorectal cancer; Sarcoma; Ovarian serous cystadenocarcinoma; Thymoma | germline | 3 | Jun 06, 2018 | clinvar |